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The Principal Biostatistician coordinates project teams, ensuring successful project completion and serving as the primary contact for clients concerning statistical matters. Responsibilities include quality control of datasets, application of advanced statistical methods, leadership in statistical reporting, and contribution to business development efforts. The role requires travel for client meetings and collaboration within a team.

The Senior Scientist I will support bioanalytical testing of samples including in-process and process development characterization. Responsibilities include method development and optimization, sample management, and compliance with laboratory safety protocols.

The Senior Data Engineer will design and implement data pipelines using Microsoft Azure services, particularly DataBricks and PowerBI, in a medallion architecture. Responsibilities include collaborating with teams, running tests, benchmarking application code, and assisting in troubleshooting during deployment across various environments.

The Project Specialist at Parexel supports project leads and team members through all project phases, ensuring proper tool setup, reporting, analysis, and financial metric collation to aid efficient project delivery.

As a Senior Biostatistician, you will lead the design and execution of statistical analysis for clinical trials, ensuring quality control of deliverables. You'll develop analysis strategies using SAS and R, mentor junior staff, and collaborate closely with study teams to impact project outcomes. Your expertise will guide protocol development and statistical reporting throughout the project life cycle.

The Site Monitor I or II will be responsible for ensuring data integrity and quality by monitoring compliance with protocols and local requirements, working closely with site managers. Responsibilities include virtual and onsite monitoring, managing complex clinical trial protocols, and collaborating with investigators and institutions.

The Site Contracts Associate will negotiate Clinical Site Agreement templates with sponsors, support budget negotiations, manage CSA activities, and liaise with project leads to ensure timely deliverables. This role also involves coordination between various stakeholders and maintaining documentation for project success.